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Clinical Manager
il y a 1 mois
Company Overview:
At EndoGene.Bio, we are revolutionizing women's health by developing high-precision diagnostic solutions for endometriosis. Our mission is to reduce the time for diagnosis from years to weeks, thanks to our proprietary biomarkers found in menstrual blood.
We are a community-driven organization that values scientific rigor, daring innovation, and kindness. We empower our team members to take ownership of their careers and strive for excellence in everything we do.
Position Overview:
As a Clinical Manager at EndoGene.Bio, you will play a critical role in driving our diagnostic solutions to market. You will collaborate with patient advocacy groups, liaise with doctors and hospital teams, develop clinical protocols, and oversee sample sourcing. Your expertise will contribute directly to the success and growth of our organization.
Key Responsibilities:
Clinical Trials & Protocols:
Develop and write clinical protocols for our diagnostic tests, ensuring adherence to regulatory requirements.
Oversee clinical studies and trials' execution, monitoring progress and identifying potential risks.
Hospital Recruitment:
Cultivate strong relationships with key opinion leaders, physicians, and hospital administrative staff.
Recruit and onboard hospitals for clinical trials, ensuring they meet all research criteria.
Patient Advocacy Engagement:
Build and maintain relationships with key patient advocacy groups related to endometriosis.
Collaborate with these groups to ensure the patient voice is central in our clinical trials and product development.
Sample Sourcing Activities:
Manage the end-to-end process of sourcing, collecting, storing, and transporting diagnostic samples.
Ensure the highest quality and integrity of samples, adhering to all regulatory and ethical standards.
Team Collaboration:
Work closely with cross-functional teams to ensure alignment on project objectives and deliverables.
Provide periodic updates and presentations to senior management on the progress of clinical projects.
Qualifications:
Medical Doctor (MD) degree, or other degrees + experience in clinical studies in IVD.
Experience in Gynaecology preferred.
Experience in clinical research or clinical project management, preferably related to diagnostics and gynaecological conditions.
Experience working with regulatory guidelines and ethical considerations in in-vitro diagnostic research.
Exceptional interpersonal and communication skills, both written and verbal.
Ability to travel as needed.
Language skills: English, French, and Spanish.
Location:
Must be based in France or Spain.
Benefits:
Competitive salary.
Comprehensive health benefits.
Company perks (if on site): transport ticket, meal tickets.
Opportunities for professional development.
Collaborative and innovative work environment.
